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Medical Device Quality Control Jobs in Nebraska (NOW HIRING)

Webforge

Quality Coordinator

Valley, NE

This position is responsible for Quality Control (QC) coordination and execution of both internal ... medical, prescription drugs, dental and vision) * 401k retirement plan with company match * Paid ...

Sotera Health

Training Specialist

Nelson, NE

... safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical ...

Sotera Health

Network Administrator

Nelson, NE · On-site

Our customers include more than 40 of the top 50 medical device companies and eight of the top ten ... and quality. We completed our initial public offering and listed our shares on the Nasdaq in ...

Sotera Health

Quality Auditor I or II

Nelson, NE · On-site

... medical device companies and 9 of the top 10 pharmaceutical companies. About the Role We are ... The Quality Auditor partners closely with laboratory personnel, Study Directors, Section Leaders ...

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How much do medical device quality control jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for medical device quality control in Nebraska is $20.48, according to ZipRecruiter salary data. Most workers in this role earn between $16.49 and $22.93 per hour, depending on experience, location, and employer.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What are popular job titles related to Medical Device Quality Control jobs in Nebraska?

For Medical Device Quality Control jobs in Nebraska, the most frequently searched job titles are:

What job categories do people searching Medical Device Quality Control jobs in Nebraska look for?

The top searched job categories for Medical Device Quality Control jobs in Nebraska are:

What cities in Nebraska are hiring for Medical Device Quality Control jobs?

Cities in Nebraska with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, and 5% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $42,589 per year, or $20.5 per hour.

Sr. Lab Operations Manager - Sterilization

Sotera Health

Nelson, NE • On-site

Full-time

Re-posted 25 days ago

Job description

The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company's unwavering commitment to its mission, Safeguarding Global Health.

Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.

Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.

Position Summary

Nelson Labs is seeking a highly strategic Senior Lab Operations Manager (Sr. LOM) to lead our Sterilization team within the laboratory operations team.

This team focuses on sterilization validation services, specifically Ethylene Oxide (EO) and steam sterilization validations for medical device and pharmaceutical products. The Sr. LOM will oversee approximately 16 employees, including 3-4 direct reports, and will play a key role in driving operational growth, technical excellence, customer satisfaction, and continuous improvement initiatives.

This role requires a leader with strong validation and operational experience who can strategically grow the business, improve efficiencies, and strengthen technical capabilities within the department.

Key Responsibilities

Operational & Technical Leadership

  • Lead daily operations for the Sterilization department
  • Oversee sterilization validation activities including EO and steam sterilization programs
  • Drive operational efficiency, turnaround time improvements, and production performance
  • Provide technical leadership in sterilization validation processes and regulatory compliance
  • Ensure laboratory resources, staffing, and workflows are optimized to support business needs

Strategic Growth & Business Partnership

  • Support departmental growth initiatives and expansion opportunities
  • Partner with Sales, Consulting, and Operations teams to enhance customer service offerings
  • Contribute to operational strategy and long-term planning initiatives
  • Drive operational excellence and process improvement efforts

Team Leadership & Development

  • Lead and mentor direct reports and laboratory personnel
  • Support employee development, succession planning, and performance management
  • Foster a collaborative, accountable, and customer-focused culture
  • Guide training program development to support technical competency and business continuity

Quality & Compliance

  • Ensure compliance with GMP, GLP, ISO, and company quality standards
  • Maintain focus on regulatory readiness, procedural adherence, and data integrity
  • Partner with Quality Assurance to address quality trends and corrective actions

Cross-Functional Collaboration

  • Work collaboratively across departments to support customer delivery and operational alignment
  • Serve as a change advocate during organizational and operational initiatives

Qualifications

Required Experience

  • Minimum 5 years of experience in:
    • Laboratory operations
    • Manufacturing or validation-focused operations
    • Leadership within regulated industries
  • Strong microbiology knowledge required
  • Hands-on laboratory experience required

Preferred Background

Strong candidates may come from:

  • Sterilization facilities
  • Medical device manufacturing
  • Validation-focused operations
  • Manufacturing leadership environments

Experience with the following is preferred:

  • Ethylene Oxide (EO) sterilization
  • Steam sterilization
  • Sterility assurance programs

Education

  • Bachelor's degree required, preferably in:
    • Biology
    • Microbiology
    • Related scientific discipline

Sotera Health goes to market through its three best-in-class businesses - Sterigenics, Nordion and Nelson Labs. Sterigenics is a leading global provider of outsourced terminal sterilization and irradiation services for the medical device, pharmaceutical, food safety and advanced applications markets. Nordion is the leading global provider of Co-60 and gamma irradiators, which are key components to the gamma sterilization process. Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.

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